|Publication number||US7722568 B2|
|Application number||US 12/021,097|
|Publication date||May 25, 2010|
|Filing date||Jan 28, 2008|
|Priority date||Jan 29, 2007|
|Also published as||US8900191, US20080183136, US20100228077|
|Publication number||021097, 12021097, US 7722568 B2, US 7722568B2, US-B2-7722568, US7722568 B2, US7722568B2|
|Inventors||Jay A. Lenker, Joseph Bishop, George F. Kick, Edward J. Nance|
|Original Assignee||Onset Medical Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (40), Referenced by (29), Classifications (9), Legal Events (3)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application claims priority to U.S. Provisional Patent Application Ser. No. 60/887,112, filed on Jan. 29, 2007, titled Expandable Intra-Aortic Balloon Pump Sheath, the entirety of which is hereby incorporated herein by reference.
1. Field of the Invention
The invention relates to medical devices for percutaneously accessing body lumens and, more particularly, to methods and devices for accessing the cardiovascular system. In one application, the invention relates to methods and devices for introducing and removing large balloon catheters and instruments, particularly intra-aortic balloon pumps, into and from a patient.
2. Description of the Related Art
A wide variety of diagnostic or therapeutic procedures involves the introduction of a device into the vasculature through a percutaneous incision at an access site. Such regions of the vasculature, preferred for access, include both the arteries and veins, typically at peripheral locations in the body. Typical access sites include the femoral arteries, and the iliac arteries. A percutaneous technique commonly known for such vascular access is the Seldinger technique. The Seldinger technique involves using a hollow needle to puncture the skin and gain access to the selected artery or vein. A guidewire is next placed through the hollow needle into the selected region of vasculature. The guidewire may be advanced to a target location in the vasculature, often more than 100 cm away from the access site. The needle is removed and a tapered dilator with a sheath and a central lumen in the dilator is advanced over the guidewire into the vasculature. The dilator is next removed and a guide catheter is advanced through the sheath over the guidewire. The guide catheter can be advanced all the way, or part way, to the target site. The guide catheter, following, or without, removal of the guidewire can be used for directing therapeutic or diagnostic catheters to regions of the vasculature and central circulation, including external and internal structures of the heart. A general objective of access systems, which have been developed for this purpose, is to minimize the cross-sectional area of the access lumen, while maximizing the available space for the diagnostic or therapeutic catheter placement therethrough. These procedures are especially suited for coronary angioplasty, stent placement, cerebrovascular coil placement, diagnostic cardiac catheterization, cardiac assist, and the like.
One type of cardiac assist procedure involves placement of an intra-aortic balloon pump (IABP) within the descending aorta of a patient and performing counterpulsation within the central circulation. The IABP procedure was originally developed by Dr. Adrian Kantrowitz in the late 1960s for use on surgical patients with the goal of improving coronary perfusion. Today, the procedure involves the steps of inserting a hollow needle, with a hemostasis valve affixed to its proximal end, into the femoral or iliac artery of a patient via a percutaneous puncture. A guidewire is next inserted through the hemostasis valve and the central lumen of the needle into the femoral or iliac artery. The guidewire is routed, under fluoroscopic control, cranially toward the heart until it reaches the aortic arch. The hollow needle is removed from the patient leaving the guidewire in place. A sheath, including a tapered tip central obturator or dilator having a hemostasis valve at its proximal end and further including a central guidewire lumen is routed over the guidewire, through the skin puncture, through the wall of the artery, and into the central lumen of the artery. The central obturator or dilator is removed. An intra-aortic balloon pump catheter is next inserted through the hemostasis valve, through the sheath, and into the artery where it is next advanced to the target site in the thoracic descending aorta. The IABP is operated to support, or augment, the patient's circulation until adequate cardiac function can be restored to allow weaning and removal of the IABP. Indications for IABP use include failure to remove from cardiopulmonary bypass, cardiogenic shock, heart failure, acute myocardial infarct, and support during high-risk interventional procedures such as percutaneous transluminal coronary angioplasty (PTCA), percutaneous heart valve placement, and coronary stent placement. The IABP is connected, at its proximal end, to a pumping and control console. An IABP pumps blood by alternate inflation and deflation within the aorta, using helium gas as the balloon inflation media, while being timed with the opening and closing of the patient's aortic valve so as to provide for optimal circulatory augmentation. Timing of the IABP cycle is generally triggered according to the patient's electrocardiogram, their blood pressure, a pacemaker (if present), or by a pre-set timer. An IABP can achieve as much as a 40% improvement in cardiac output with accompanying reductions in left ventricular stroke work and myocardial oxygen consumption. The IABP can be left in place for periods of hours to more than 2 weeks to allow restoration of natural cardiac function. The IABP can be removed from the patient by first deflating the balloon and then withdrawing the IABP until it is removed from the patient. The sheath is next removed and hemostasis is established using standard techniques for a vessel puncture wound.
Issues can arise, however, when the IABP is removed from the patient. Following deflation, the collapsed balloon, typically fabricated from a thin layer of inelastic polyethylene, may form a plurality of wings, or flattened, radially outwardly projecting structures that are relatively hard and sharp and may not fold neatly against the catheter shaft. Such balloon wings have been reported to cause disruption of vessel plaque during removal or pullback through the aorta, iliac and femoral arteries. This is especially problematic in very sick patients with significant vascular disease that involves plaque, mural thrombus, aneurysms, and other pathologies. The disruption of a region of plaque or thrombus can cause emboli to break free from the vessel wall, float downstream, and lodge within the lumen of smaller distal vessels, blocking blood flow, and resulting in ischemia and possibly tissue necrosis.
Suggested further reading related to the use of intra-aortic balloon pumps includes P. J. Overwalder: “Intra Aortic Balloon Pump (IABP) Counterpulsation”, The Internet Journal of Thoracic and Cardiovascular Surgery, 1999, Volume 2 Number 2 and “Counterpulsation: Historical Background, Technical Improvements, Hemodynamic and Metabolic Effects”, Cardiology, Volume 84, 1994, pp. 156-167.
It is desirable to protect the arteries, including the femoral and iliac arteries, from the IABP during removal. A need remains, therefore, for improved access technology, which allows a large diameter balloon catheter to be percutaneously or surgically introduced, endovascularly advanced to the descending aorta, pumped for a period of hours, days, or weeks, and then be removed without causing further injury or complications to the patient.
A transluminal, radially expanding access sheath is provided according to an embodiment of the invention. In an embodiment, the radially expanding sheath, or introducer, is used to provide access to the mammalian aorta by way of a femoral or iliac artery puncture and advancement retrograde toward the aortic arch through the arterial system. The mammalian aorta can be that of a human or human patient. A distal portion of the introducer or sheath is collapsed radially to minimize its outside diameter. A portion of the introducer or sheath, therefore, has a first, smaller cross-sectional profile that can be dilated to a second, larger cross-sectional profile. The catheter, introducer, or sheath can enter a vessel or body lumen with a diameter of 3 to 12 French or smaller, and allow passage of instruments through a central lumen that is 2 to 10 French. At the conclusion of the procedure, the sheath or catheter is capable of gently dilating its entire collapsed length, which can be a small portion of, or substantially the entire working length of the sheath or introducer. The sheath, introducer, or catheter, when expanded, can dilate the arterial puncture site using radially outwardly directed force and permit the removal of instrumentation therethrough, even when that instrumentation is large and unfurled. The sheath or catheter can be maximally visible under fluoroscopy and can be relatively inexpensive to manufacture. The sheath, catheter, or introducer can be kink-resistant and provide a stable or stiff platform for large catheter introduction therethrough.
In an embodiment, the sheath can have an introduction outside diameter that ranges from 3 to 15 French with a preferred range of 5 to 12 French. The inside diameter of the sheath can be expandable to permit instruments ranging up to 30 French to pass therethrough, with a preferred range of between 3 and 20 French. The sheath can have a working length ranging between 20-cm and 200-cm with a preferred length of 50-cm to 150-cm. The expandable distal end of the catheter can comprise between 5% and 95% of the overall working length of the catheter. The outside diameter of the proximal end of the catheter is generally larger than the outside diameter of the expanded distal end, due to increased wall thickness and reinforcement, to provide for pushability, torqueability (preferably approximately 1:1 torqueability), steerability, control, column strength, and the ability to easily pass large diameter instruments therethrough. In an embodiment, the sheath or introducer can be routed to its destination over one or more already placed guidewires with a diameter ranging from 0.010 inches up to 0.050 inches and generally approximating 0.032 to 0.038 inches in diameter.
An embodiment of the invention comprises an endovascular access system further comprising an axially elongate tubular body that defines a lumen extending from the proximal end to the distal end of the sheath. At least a portion of the elongate tubular body is expandable from a first, smaller cross-sectional profile to a second, greater cross-sectional profile. In an embodiment, the first, smaller cross-sectional profile is created by creating axially oriented folds in the sheath material. The expandable region can be the distal end, the proximal end, or both. These folds may be located in only one circumferential position on the sheath, or there may be a plurality of such folds or longitudinally oriented crimps in the sheath. The folds or crimps may be made permanent or semi-permanent by heat-setting the structure, once folded. In an embodiment, a releasable or expandable jacket is carried by the access sheath to restrain at least a portion of the elongate tubular structure in the first, smaller cross-sectional profile during insertion and up to or during inflation of the distal region. In another embodiment, the jacket is replaced by a packaging aid that is removed prior to inserting the sheath into the patient. In an embodiment, the elongate tubular body is sufficiently pliable to allow the passage of objects having a single maximum cross-sectional dimension larger than an inner diameter of the elongate tubular body in the second, greater cross-sectional profile. The adaptability to objects of larger dimension is accomplished by pliability or re-shaping of the cross-section to the larger dimension in one direction accompanied by a reduction in dimension in a lateral direction. The adaptability may also be generated through the use of malleable or elastomerically deformable sheath material. This re-shaping or non-round cross-section can be beneficial in passing two or more catheters through a single sheath with a minimum lateral cross-sectional area.
In another embodiment of the invention, a transluminal access sheath assembly for providing minimally invasive access comprises an elongate tubular member having a proximal end and a distal end and defining a working inner lumen. In this embodiment, the tubular member comprises a folded or creased sheath that can be expanded by a dilatation balloon catheter. The dilatation balloon, affixed to the dilatation balloon catheter, if filled with fluids, preferably liquids and further preferably radiopaque liquids, at appropriate pressure, can generate the necessary force to radially dilate or expand the sheath. The dilatation balloon catheter is removable to permit subsequent instrument or catheter passage through the sheath. The sheath wall can be constructed of malleable materials so that the sheath retains its shape before and after balloon expansion. Such malleable construction can include polymeric walls with metallic coils, braids, meshes, stents, or other reinforcement embedded therein. Longitudinal runners may be disposed within the sheath to serve as tracks for instrumentation, which further minimize friction while minimizing the risk of catching the instrument on the expandable plastic tubular member. Such longitudinal runners are preferably circumferentially affixed within the sheath so as not to shift out of alignment. In yet another embodiment, the longitudinal runners may be replaced by longitudinally oriented ridges and valleys, termed flutes. The flutes, or runners, can be oriented along the longitudinal axis of the sheath, or they can be oriented in a spiral, or rifled, fashion.
In an embodiment, the proximal end of the access assembly, apparatus, or device is preferably fabricated as a structure that is flexible, resistant to kinking, and further retains both column strength and torqueability. Such structures include tubes fabricated with coils or braided reinforcements and preferably comprise inner walls that prevent the reinforcing structures from protruding, poking through, or becoming exposed to the inner lumen of the access apparatus. Such proximal end configurations may be single lumen, or multi-lumen designs, with a main lumen suitable for instrument, guidewire, endoscope, or obturator passage and additional lumens being suitable for control and operational functions such as balloon inflation. Such proximal tube assemblies can be affixed to the proximal end of the distal expandable segments described heretofore.
In an embodiment, the sheath can comprise an inner layer of thin polymeric material, an outer layer of polymeric material, and a central region comprising a coil, braid, stent, plurality of hoops, or other reinforcement. It is beneficial to create a bond between the outer and inner layers at a plurality of points, most preferably at the interstices or perforations in the reinforcement structure, which is generally fenestrated. Such bonding between the inner and outer layers causes a braided structure to lock in place. In another embodiment, the inner and outer layers are not fused or bonded together in at least some, or all, places. When similar materials are used for the inner and outer layers, the sheath structure can advantageously be fabricated by fusing of the inner and outer layer to create a uniform, non-layered structure surrounding the embedded reinforcement. The polymeric materials used for the outer wall of the jacket are preferably elastomeric to maximize flexibility of the catheter. The polymeric materials used in the composite catheter inner wall may be the same materials as those used for the outer wall, or they may be different. In another embodiment, a composite tubular structure can be co-extruded by extruding a polymeric compound with a stent, braid, or coil structure embedded therein. The reinforcing structure is preferably fabricated from annealed metals, such as fully annealed stainless steel, titanium, or the like. In this embodiment, once expanded, the folds or crimps can be held open by the reinforcement structure embedded within the sheath, wherein the reinforcement structure is malleable but retains sufficient force to overcome any forces imparted by the sheath tubing.
In an embodiment, the sheath is inserted into the patient in its collapsed configuration. In this embodiment, a therapeutic balloon catheter is pre-inserted through the collapsed central lumen of the sheath so that the therapeutic balloon projects distally of the collapsed expandable region of the introducer. The therapeutic balloon catheter, which comprises the large diameter balloon, also comprises inflation lumens allowing for pulsatile, repeated inflation-deflation cycles of the large diameter balloon such as found in an intra aortic balloon pump. The therapeutic balloon catheter can comprise a secondary sheath expansion device such as a coaxially-mounted angioplasty-type balloon that is furled and can be inserted inside the collapsed, non-expanded sheath. The introducer, or its dilator, can comprise a lead in sheath, which is small in diameter and passes percutaneously into the vasculature during the majority of the time during which the therapeutic balloon catheter functions. Following completion of the therapy, an example of which is intra-aortic balloon counterpulsation, the lead in sheath is either split and peeled away, or advanced with the dilator to introduce the expandable portion of the sheath into the patient's vasculature. Following operation of the intra aortic balloon pump, the large diameter balloon is deflated and the secondary sheath expansion device is activated to expand the sheath to a large diameter. The secondary sheath expansion device, which can be a balloon, is deactivated or deflated and the entire therapeutic balloon catheter can now be safely withdrawn within the sheath and removed from the patient without concern for the edges of the deflated large diameter balloon coming in contact with the patient's vessel walls. The sheath can now be removed from the patient either fully expanded or following collapse of the expandable region.
In an embodiment of the invention, it is beneficial that the sheath comprise a radiopaque marker or markers. The radiopaque markers may be affixed to the non-expandable portion or they may be affixed to the expandable portion. Markers affixed to the radially expandable portion preferably do not restrain the sheath or catheter from radial expansion or collapse. Markers affixed to the non-expandable portion, such as the catheter shaft of a balloon dilator can be simple rings that are not radially expandable. Radiopaque markers include shapes fabricated from malleable material such as gold, platinum, tantalum, platinum-iridium, and the like. Radiopacity can also be increased by vapor deposition coating or plating metal parts of the catheter with metals or alloys of gold, platinum, tantalum, platinum-iridium, and the like. Expandable markers may be fabricated as undulated or wavy rings, bendable wire wound circumferentially around the sheath, or other structures such as are found commonly on stents, grafts, stent-grafts, or catheters used for endovascular access in the body. Expandable radiopaque structures may also include disconnected or incomplete surround shapes affixed to the surface of a sleeve or other expandable shape. Non-expandable structures include circular rings, bands, cylinders, or other structures that completely surround the catheter circumferentially and are strong enough to resist expansion. In another embodiment, the polymeric materials of the catheter or sheath may be loaded with radiopaque filler materials such as, but not limited to, bismuth salts, or barium salts, or the like, at percentages ranging from 1% to 50% by weight in order to increase radiopacity. The radiopaque markers allow the sheath to be guided and monitored using fluoroscopy.
In order to enable radial or circumferential expansive translation of the reinforcement, it may be beneficial not to completely bond the inner and outer layers together, thus allowing for some motion of the reinforcement in translation as well as the normal circumferential expansion. Regions of non-bonding may be created by selective bonding between the two layers or by creating non-bonding regions using a slip layer fabricated from polymers, ceramics or metals. Radial expansion capabilities are important because the proximal end needs to transition to the distal expansive end and, to minimize manufacturing costs, the same catheter may be employed at both the proximal and distal end, with the expansive distal end undergoing secondary operations to permit radial, or diametric, expansion.
In another embodiment, the distal end of the catheter is fabricated using an inner tubular layer, which is thin and lubricious. This inner layer is fabricated from materials such as, but not limited to, FEP, PTFE, polyamide, polyethylene, polypropylene, Pebax, Hytrel, and the like. The reinforcement layer comprises a coil, braid, stent, or plurality of expandable, foldable, or collapsible rings, which are generally malleable and maintain their shape once deformed. Preferred materials for fabricating the reinforcement layer include but are not limited to, stainless steel, tantalum, gold, platinum, platinum-iridium, titanium, nitinol, and the like. The materials are preferably fully annealed or, in the case of nitinol, fully martensitic. The outer layer is fabricated from materials such as, but not limited to, FEP, PTFE, polyamide, polyethylene, polypropylene, polyurethane, Pebax, Hytrel, and the like. The inner layer is fused or bonded to the outer layer through holes in the reinforcement layer to create a composite unitary structure. The structure is crimped radially inward to a reduced cross-sectional area. A balloon dilator is inserted into the structure before crimping or after an initial crimping and before a final sheath crimping. The balloon dilator is capable of forced radial, or diametric, expansion of the reinforcement layer, which provides sufficient strength necessary to overcome any forces imparted by the polymeric tubing, thus controlling the cross-sectional shape of the polymeric tubing. The dilator is also capable of overcoming any forces imparted by tissues, including atrial or even ventricular myocardial tissue, through which the sheath is inserted.
Another embodiment of the invention comprises a method of providing endovascular protection for vascular or arterial structures through which an intra-aortic balloon pump catheter is passed. The method first comprises percutaneously placing a hollow needle into the femoral artery, inserting a guidewire through the hollow needle into the artery, withdrawing the hollow needle, and inserting a sheath with a tapered obturator into the puncture site and into the artery over the guidewire. The guidewire is next withdrawn, as is the tapered obturator and a 0.032 to 0.038-inch guidewire, preferably a stiff or super-stiff guidewire, is advanced into the artery and approximately to the level of the aortic arch. The IABP catheter, having a shaft that is 5 to 10 French in diameter, pre-inserted within the lumen of a radially expandable sheath is next advanced into the femoral artery and advanced to the top of the descending aorta over the guidewire. The guidewire is optionally withdrawn or it may be retained in place. The expandable sheath is maintained collapsed and in position just proximal to the balloon of the IABP. The IABP is operated for a period of hours to weeks, wherein the large diameter balloon, which is 20 to 40 mm diameter, is repeatedly expanded and collapsed, under fluid pressure, to cause volumetric change within the aorta, in synchronization with the patient's heart. Such expansion and contraction cycles can occur at a rate of between 40 and 200 beats per minute. A sheath dilator, positioned within the expandable sheath and optionally integral to the IABP catheter shaft, is next radially expanded, forcefully causing the sheath, or its distal end, to expand radially so as to dilate the expandable portion of the sheath. The dilator is next deflated along with the IABP balloon and the entire assembly is removed from the sheath. Alternatively, the IABP balloon catheter is withdrawn sufficiently to shield the collapsed IABP balloon from the blood vessel walls. The sheath is configured to re-fold or compress the IABP balloon prior to removal so that when the IABP balloon is pulled out of the arteries, the artery walls are protected. Suitable hemostatic and anti-reflux valves and seals are affixed the distal end of all devices except guidewires to ensure maintenance of hemostasis and prevention of air entry into the vasculature. Following therapeutic or diagnostic procedures, or both, the sheath is withdrawn from the patient allowing the arterial puncture to close.
The expandable access sheath is configured, or tailored, to bend, or flex, around vascular tortuosity and be advanced into the aorta through potentially tortuous iliac and femoral arteries. Provision can optionally be made to actively orient or steer the sheath through the appropriate angles of between 20 to 120 degrees or more and to bend in one or even two planes of motion. The steering mechanism, in various embodiments, can be a curved guidewire and straight catheter, curved catheter and straight guidewire, a movable core guidewire, or a combination of the aforementioned. In one embodiment, radial expansion of the distal end of the access sheath from a first, smaller diameter cross-section to a second larger diameter cross-section is next performed, using a balloon dilator. The balloon dilator is subsequently removed from the sheath to permit passage of instruments that may not normally have been able to be inserted into the vasculature. Once the sheath is in place, the guidewire may be removed or, in another embodiment, it may be left in place.
In another embodiment of the invention, the expandable sheath is not pre-mounted to the therapeutic balloon catheter. Instead, the expandable sheath is configured so that it retains an internal lumen, even in its collapsed, first smaller cross-sectional configuration, such that the therapeutic balloon catheter can be inserted therethrough. In this embodiment, the collapsed sheath is inserted into the circulatory system with a central obturator and nose cone over a guidewire. The obturator is removed and the therapeutic balloon catheter is inserted through the collapsed sheath and into the circulatory system. The therapeutic balloon catheter is cyclically inflated and deflated for a period of time, following which it is finally deflated. A sheath dilation catheter is next inserted into the collapsed portion of the sheath. The sheath dilatation catheter is inflated to expand the first, smaller cross-sectional area to a second, larger cross-sectional area. The sheath dilatation catheter is deflated and removed from the sheath, following which the deflated therapeutic balloon catheter is withdrawn into the sheath so that it is shielded from outside tissue. The entire sheath is next removed from the patient, with or without the therapeutic balloon catheter having been entirely removed from the expandable sheath.
In another embodiment of the invention, the proximal end of the expandable sheath comprises hemostasis or backflow check seals or valves to prevent blood loss and retrograde flow of air into the circulatory system. The hub of the sheath comprises such a hemostasis seal. The seal comprises an annular soft elastomeric gasket that seals against catheters, instruments, and the dilator, inserted therethrough. The seal can further comprise a valve such as a stopcock, a hemostasis valve, a one-way valve such as a duckbill or flap valve, or the like to prevent significant blood loss and air entry when an instrument or catheter is removed from the lumen of the expandable sheath. The soft annular seal can further comprise a mechanism to compress the inner diameter of the seal radially inward, such as the mechanisms found on Tuohy-Borst valves. The hub further comprises one or more sideport for injection of contrast media such as OmnipaqueŽ, RenografinŽ, or other Barium-loaded solutions, for example, saline, or anticoagulant solutions such as warfarin, heparin, CoumadinŽ, persantin, or the like, or for the measurement of pressure at or near the distal end of the sheath. The dilator hub comprises a central lumen with a Tuohy-Borst valve and one or more sideports for balloon inflation, said sideports operably connected to lumens in the dilator catheter for injection or withdrawal of fluids from a balloon at the distal end of the dilator and optionally for measurement of pressure at or near the dilator distal end. The dilator hub, the sheath hub, or both, can also comprise a handle, lever, or trigger mechanism to enable steering mechanisms at the distal end of the dilator, the sheath, or both, respectively.
The expandable sheath, in an embodiment, comprises radiopaque markers to denote the beginning, and end, of the expandable region and the middle of the expandable region. The middle of the expandable region is useful in that it can be aligned with the atrial septum during the sheath expansion procedure. The sheath can comprise radiopaque materials such as gold wire, platinum wire, tantalum wire, or coatings of the aforementioned over a malleable, stainless steel, deformable reinforcing layer. Such complete radiopaque markings are especially useful for sheath dilation insofar as they allow the operator to more clearly visualize the extent to which the sheath has been dilated once the dilator is activated. In a preferred embodiment, a radiopaque marker band is affixed to the dilator substantially near the distal tip of the dilator so that the position of the distal tip can be observed and controlled relative to the wall of the aorta or other cardiac structures. This radiopaque marker band can be a non-expandable, axially elongate tubular structure that is adhered to the non-expandable dilator shaft. Another non-expandable radiopaque marker band can be adhered to the dilator shaft at a position substantially corresponding to the proximal most dilating portion of the dilator or sheath. Another non-expandable radiopaque marker band can be adhered to the dilator shaft at a position substantially corresponding to the distal most dilating portion of the dilator or sheath. The radiopaque marker bands can further be configured to appear different under fluoroscopy, for example by making the distal tip marker a single band, the distal dilation marker two bands, and the proximal dilator marker, three bands. Yet another configuration of radiopaque marker bands can be achieved by using malleable wire windings of gold, tantalum, platinum alloys, or the like, which are embedded within the folded and expandable sheath, preferably at or near the distal end of the sheath and, optionally, at or near the proximal end of the expandable portion of the sheath. These wire windings can expand with the sheath and can help show the extents of the sheath even after the dilator has been removed.
In an embodiment, the sheath dilator or expander is a separate catheter from the therapeutic or diagnostic catheter and which can be removed or advanced separately from the therapeutic or diagnostic catheter. In another embodiment, the sheath dilator is affixed to or integral to the therapeutic or diagnostic catheter. In this latter embodiment, the sheath dilator can be an angioplasty-type, non-elastomeric balloon affixed to the therapeutic or diagnostic catheter at a location proximal to the therapeutic or diagnostic mechanisms at the distal end of the catheter. The inflation lumen for the sheath expansion dilator balloon is separate from that of the inflation lumen for the therapeutic or diagnostic device at the distal end of the catheter. These sheath expansion lumen and the therapeutic working lumen can run the length of the catheter and are operably connected to and generally terminate at ports at the proximal end of the catheter, for example on a hub, Y-connector, or other structure. At its distal end, the sheath expansion lumen is operably connected with the interior volume of the sheath expansion balloon. The sheath expansion lumen does not continue to and vent from the distal end of the catheter. The therapeutic working lumen or therapeutic balloon inflation lumen generally terminates at, and is operably connected with, the volume described by the interior of the therapeutic balloon. In an exemplary case, the therapeutic or diagnostic balloon is an intra-aortic balloon pump.
In another embodiment, the proximal end of the sheath comprises a non-circular interior cross-section. The interior cross-section of the sheath can be oval, or it can comprise two or more completely walled off or partially walled off separate lumens. The sheath hub, which is affixed to the non-expandable proximal end of the sheath, can comprise two or more separate instrumentation ports, each of which are operably connected to a lumen or partial lumen within the sheath and which can advantageously comprise hemostasis valves, sealing gaskets, or the like. The instrumentation ports are especially useful for passage of, for example, multiple catheters. Segregation of the multiple catheters can be useful to prevent binding or interference between the multiple catheters or instruments passed through the sheath. In yet another embodiment, the proximal end of the sheath has a non-circular cross-section that minimizes the overall cross-sectional area or circumference of a sheath configured to accept two or more catheters. This non-circular cross-section can be an oval, ellipse, rounded triangle, or the like. The non-circular cross section can, for example, reduce an 18 French OD catheter to around 15.5 French, using the same wall thickness and still retain the capability to accept two 8 French catheters within its internal lumen or lumens. Reduction in exterior cross-section is clearly useful in making the procedure as minimally invasive as possible and may make a procedure, which normally takes a cutdown, a percutaneous procedure.
In another embodiment, the guidewire port on the dilator hub is operably connected to a sideport. The sideport further comprises a flexible line and a luer connector and may further comprise an optional stopcock or one way valve. The sideport can be a T-fitting, a Y-fitting, or it can be integrally molded with the guidewire port on the dilator hub. The sideport can accept catheters or instruments for the purpose of, for example, taking pressure or flow rate measurements. The guidewire port is preferably terminated at its proximal end with a Tuohy-Borst fitting, hemostasis valve, ring gasket, or other valve or seal system. In yet another embodiment, the exterior of the sheath, and optionally the internal lumen of the sheath, can be coated with a lubricious coating comprising materials such as, but not limited to, silicone oil or a hydrophilic hydrogel. The dilator hub can further comprise one or more irrigation, aspiration, or purge port operably connected to the guidewire lumen and preferably terminated with a stopcock. Such irrigation, aspiration, or purge port can also be affixed to the sheath hub and be operably connected to the central lumen of the expandable sheath. In yet another embodiment, the expandable sheath can comprise an outer sleeve which surrounds the sheath and dilator and provides an aseptic barrier during the insertion and therapeutic function of the central catheter, such therapeutic function including, but not limited to, intra-aortic balloon counterpulsation. The outer sleeve can further comprise seals at one or both ends to facilitate sheath or catheter function while maximizing the protective function of the outer sleeve.
For purposes of summarizing the invention, certain aspects, advantages and novel features of the invention are described herein. It is to be understood that not necessarily all such advantages may be achieved in accordance with any particular embodiment of the invention. Thus, for example, those skilled in the art will recognize that the invention may be embodied or carried out in a manner that achieves one advantage or group of advantages as taught herein without necessarily achieving other advantages as may be taught or suggested herein. These and other objects and advantages of the present invention will be more apparent from the following description taken in conjunction with the accompanying drawings.
A general architecture that implements the various features of the invention will now be described with reference to the drawings. The drawings and the associated descriptions are provided to illustrate embodiments of the invention and not to limit the scope of the invention. Throughout the drawings, reference numbers are re-used to indicate correspondence between referenced elements.
The invention may be embodied in other specific forms without departing from its spirit or essential characteristics. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is therefore indicated by the appended claims rather than the foregoing description. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.
The invention, which can be generally termed a catheter or a sheath, can be described as being an axially elongate hollow tubular structure having a proximal end and a distal end. The axially elongate structure further has a longitudinal axis and has an internal through lumen that extends from the proximal end to the distal end for the passage of instruments, fluids, tissue, or other materials. The axially elongate hollow tubular structure is generally flexible and capable of bending, to a greater or lesser degree, through one or more arcs in one or more directions perpendicular to the main longitudinal axis. As is commonly used in the art of medical devices, the proximal end of the device is the end that is closest to the user, typically a cardiologist, surgeon, or electrophysiologist. The distal end of the device is the end closest to the patient or that is first inserted into the patient. A direction being described as being proximal to a certain landmark will be closer to the user, along the longitudinal axis, and further from the patient than the specified landmark. The diameter of a catheter is often measured in “French Size” which can be defined as 3 times the diameter in millimeters (mm). For example, a 15 French catheter is 5 mm in diameter. The French size is designed to approximate the circumference of the catheter in mm and is often useful for catheters that have non-circular cross-sectional configurations. While the original measurement of “French” used π (3.14159 . . . ) as the conversion factor between diameters in millimeters (mm) and French, the system has evolved today to where the conversion factor is 3.0.
In an embodiment, the IABP catheter 530 moves axially in concert with the dilator 528, although 1 to 1 motion is not required and axial relative motion between the IABP catheter 530 and the dilator 528 can be beneficial for making position adjustments of the IABP catheter 530 when the sheath 532 and dilator 528 are located appropriately. The entire system 500 is typically advanced over an already placed guidewire to a target location in the vasculature, for example in the thoracic aorta, in the configuration shown in
The sterile barrier 640 surrounds the outside diameter of the sheath 632 and is affixed at its proximal end to the proximal sterile seal 644. The sterile barrier 640 is affixed at its distal end to the distal sterile seal 642. The sterile barrier 640 can be configured to telescope, accordion, or otherwise accommodate axial or longitudinal shortening. The sterile barrier 640 and the proximal and distal seals 644 and 642 comprise structures that prevent migration of microbes across their boundaries. The proximal seal 644 can be affixed to the proximal portion 504 of the sheath 632 or it can be affixed to the sheath hub 502. In another embodiment, the proximal seal 644 can be slidably movable along the longitudinal axis of the proximal portion 504 but always maintains a complete, or nearly complete, sterile barrier by means of a seal. The seal can be achieved using a soft elastomeric gasket, O-ring, or the like. The slidability can be enhanced by means of lubricious materials in the proximal seal 644 or the proximal portion 504 such as, but not limited to, PTFE, FEP, polyethylene, hydrogel, polypropylene, silicone lubricants, or the like. The distal seal 642 can be slidably movable along the longitudinal axis of the distal portion 506 of the sheath 632. The distal seal 642 is configured to maintain a complete, or nearly complete, sterile seal against the distal portion 506. The distal seal 642 can be configured similarly to the proximal seal 644 using similar materials. The distal seal 642, however, seals against an outer surface 506 which is not complete and unbroken, but which can comprise one or more longitudinal fold. Thus, the distal seal 642 can be comprised, on its internal aspect of gap-filling, swellable material such as open or closed cell foam, hydrogel, or very soft elastomer such as, but not limited to, thermoplastic elastomer or silicone elastomer with a durometer of 5 A to 30 A. The distal seal 642 can be thicker than the proximal seal 644 and can be pre-compressed to a greater extent than that of the proximal seal 644 to permit accommodation of uneven sheath exterior contours, as well as to accommodate for radial expansion of the distal region 506 in the range of about 1.2× to about 5× its original radius. The length of the sterile barrier 640 can range from about 1-cm to about 90-cm and preferably range from about 10-cm to about 50-cm.
Aspects of the invention include the methods of use of the IABP sheath in conjunction with an IABP catheter and pumping system. The IABP catheter is used in conjunction with an IABP pumping system. The balloon inflation port near the proximal end of the IABP catheter is operably connected to the outlet of the IABP pumping system, generally by way of a connector line. The IABP pumping system is a pulsatile device that generates and then relieves pressure at its outlet at a rate that is set on the console or is driven from a trigger circuit operably connected to an electrocardiogram (ECG) measuring device which acquires electrocardiogram data from the patient. The IABP pumping system is generally a piece of hardware that is situated on a roll-around cart or on a stand near the patient. The gas generally used for pumping the IABP pumping balloon is helium, although carbon dioxide or other gasses may be considered suitable. The choice of gas is generally made based on the ability of the gas to dissipate if it leaks into the cardiovascular system, although the viscosity of the gas is important in designing the smallest possible diameter IABP catheter.
The present invention may be embodied in other specific forms without departing from its spirit or essential characteristics. For example, the sheath may include instruments affixed integrally to the interior central lumen of the sheath, rather than being separately inserted, for performing therapeutic or diagnostic functions. The sheath hub may comprise tie downs or configuration changes to permit attaching the hub to the mouth, nose, or face of the patient. The dilatation means may be a balloon dilator as described in detail herein, or it may be a translation dilator wherein an inner tube is advanced longitudinally to expand an elastomeric small diameter tube. The sheath or introducer described herein can be used for other large therapeutic catheters including those, for example, intended to perform balloon valvuloplasty. Various valve configurations and radiopaque marker configurations are appropriate for use in this device. The IABP catheter can be longitudinally affixed to the dilator or it can be slidably constrained relative to the dilator. The described embodiments are to be considered in all respects only as illustrative and not restrictive. The scope of the invention is therefore indicated by the appended claims rather than the foregoing description. All changes that come within the meaning and range of equivalency of the claims are to be embraced within their scope.
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|U.S. Classification||604/164.03, 604/96.01, 604/4.01|
|International Classification||A61M29/00, A61M5/178, A61M37/00|
|Cooperative Classification||A61M25/0662, A61M2025/0024|
|Mar 18, 2008||AS||Assignment|
Owner name: ONSET MEDICAL CORPORATION, CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LENKER, JAY A.;BISHOP, JOSEPH;KICK, GEORGE F.;AND OTHERS;REEL/FRAME:020671/0928;SIGNING DATES FROM 20080213 TO 20080313
Owner name: ONSET MEDICAL CORPORATION,CALIFORNIA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:LENKER, JAY A.;BISHOP, JOSEPH;KICK, GEORGE F.;AND OTHERS;SIGNING DATES FROM 20080213 TO 20080313;REEL/FRAME:020671/0928
|Nov 16, 2010||CC||Certificate of correction|
|Sep 25, 2013||FPAY||Fee payment|
Year of fee payment: 4